Uncialamycin-based antibody-drug conjugates: Unique enediyne ADCs exhibiting bystander killing effect.


Journal

Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876

Informations de publication

Date de publication:
22 06 2021
Historique:
entrez: 22 6 2021
pubmed: 23 6 2021
medline: 15 12 2021
Statut: ppublish

Résumé

Antibody-drug conjugates (ADCs) have emerged as valuable targeted anticancer therapeutics with at least 11 approved therapies and over 80 advancing through clinical trials. Enediyne DNA-damaging payloads represented by the flagship of this family of antitumor agents,

Identifiants

pubmed: 34155147
pii: 2107042118
doi: 10.1073/pnas.2107042118
pmc: PMC8237573
pii:
doi:

Substances chimiques

Anthraquinones 0
Immunoconjugates 0
uncialamycin 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Déclaration de conflit d'intérêts

The authors declare no competing interest.

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Auteurs

K C Nicolaou (KC)

BioScience Research Collaborative, Department of Chemistry, Rice University, Houston, TX 77005; kcn@rice.edu julia.gavrilyuk@gmail.com.

Stephan Rigol (S)

BioScience Research Collaborative, Department of Chemistry, Rice University, Houston, TX 77005.

Emmanuel N Pitsinos (EN)

BioScience Research Collaborative, Department of Chemistry, Rice University, Houston, TX 77005.
Laboratory of Natural Products Synthesis & Bioorganic Chemistry, Institute of Nanoscience and Nanotechnology, National Centre for Scientific Research "Demokritos", 153 10 Agia Paraskevi, Greece.

Dipendu Das (D)

BioScience Research Collaborative, Department of Chemistry, Rice University, Houston, TX 77005.

Yong Lu (Y)

BioScience Research Collaborative, Department of Chemistry, Rice University, Houston, TX 77005.

Subhrajit Rout (S)

BioScience Research Collaborative, Department of Chemistry, Rice University, Houston, TX 77005.

Alexander W Schammel (AW)

Discovery Chemistry Department, AbbVie Inc., South San Francisco, CA 94080.

Dane Holte (D)

Discovery Chemistry Department, AbbVie Inc., South San Francisco, CA 94080.

Baiwei Lin (B)

Bioconjugation and Process Development Department, AbbVie Inc., South San Francisco, CA 94080.

Christine Gu (C)

Bioconjugation and Process Development Department, AbbVie Inc., South San Francisco, CA 94080.

Hetal Sarvaiya (H)

Bioconjugation and Process Development Department, AbbVie Inc., South San Francisco, CA 94080.

Jose Trinidad (J)

Bioconjugation and Process Development Department, AbbVie Inc., South San Francisco, CA 94080.

Nicole Barbour (N)

Bioconjugation and Process Development Department, AbbVie Inc., South San Francisco, CA 94080.

Amanda M Valdiosera (AM)

Bioconjugation and Process Development Department, AbbVie Inc., South San Francisco, CA 94080.

Joseph Sandoval (J)

Assay Development Department, AbbVie Inc., South San Francisco, CA 94080.

Christina Lee (C)

Assay Development Department, AbbVie Inc., South San Francisco, CA 94080.

Monette Aujay (M)

Assay Development Department, AbbVie Inc., South San Francisco, CA 94080.

Hanan Fernando (H)

Cancer Biology Department, AbbVie Inc., South San Francisco, CA 94080.

Anukriti Dhar (A)

Cancer Biology Department, AbbVie Inc., South San Francisco, CA 94080.

Holger Karsunky (H)

Cancer Biology Department, AbbVie Inc., South San Francisco, CA 94080.

Nicole Taylor (N)

In Vivo Pharmacology Department, AbbVie Inc., South San Francisco, CA 94080.

Marybeth Pysz (M)

In Vivo Pharmacology Department, AbbVie Inc., South San Francisco, CA 94080.

Julia Gavrilyuk (J)

Discovery Chemistry Department, AbbVie Inc., South San Francisco, CA 94080; kcn@rice.edu julia.gavrilyuk@gmail.com.

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Classifications MeSH